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Ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is a chemical compound with the molecular formula C8H12N2O2. It belongs to the category of pyrazoles, which are organic compounds characterized by a five-membered aromatic ring containing two nitrogen atoms in nonadjacent positions. ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is known for its chemical stability and is primarily used in chemical synthesis and pharmaceutical applications. Its synthesis typically involves the reaction of ethyl chloroformate with 1,4-dimethylpyrazole. Due to its potentially hazardous nature, it is essential to consider safety measures when handling this substance.

68809-65-4

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68809-65-4 Usage

Uses

Used in Chemical Synthesis:
Ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is used as an intermediate in the synthesis of various chemical compounds. Its stability and reactivity make it a valuable component in the production of a range of products.
Used in Pharmaceutical Applications:
Ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is used as a building block in the development of pharmaceutical drugs. Its unique structure and properties contribute to the creation of new and effective medications for various medical conditions.
Used in Research and Development:
Ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is used as a research compound in the study of pyrazole chemistry and its potential applications in various fields, including materials science and drug discovery.
Used in Safety and Handling:
Ethyl 1,4-dimethyl-1H-pyrazole-3-carboxylate is used as a reference material for understanding the safety measures and handling procedures required when working with potentially hazardous chemical substances. This knowledge is crucial for ensuring the safe use and disposal of such compounds in both industrial and laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 68809-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,0 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68809-65:
(7*6)+(6*8)+(5*8)+(4*0)+(3*9)+(2*6)+(1*5)=174
174 % 10 = 4
So 68809-65-4 is a valid CAS Registry Number.

68809-65-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1,4-dimethylpyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl-1,4-ethoxycarbonyl-3-pyrazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:68809-65-4 SDS

68809-65-4Relevant academic research and scientific papers

AMIDO COMPOUNDS AS AhR MODULATORS

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Paragraph 0695; 0703, (2019/02/06)

Provided herein are compounds, compositions and methods of using the compounds and compositions for the treatment of diseases modulated, as least in part, by AhR. The compounds are represented by formulae Formula (I), (II), (III), (iv): wherein the letters and symbols a, b, c, d, e, f, g, Z, R1b, R2a and R2b have the meanings provided in the specification.

PYRAZOLYL-BASED CARBOXAMIDES AS CRAC INHIBITORS

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Page/Page column 34, (2016/04/26)

The invention relates to pyrazolyl-based carboxamide compounds useful as ICRAC inhibitors, to pharmaceutical compositions containing these compounds and to these compounds for the use in the treatment and/or prophylaxis of diseases and/or disorders, in particular inflammatory diseases and/or inflammatory disorders.

Haloacetylated enol ethers. 11 [16]. Synthesis of 1-methyl- and 1- phenyl pyrazole-3(5)-ethyl esters. A one-pot procedure

Martins, Marcos A. P.,Freitag, Rogerio A.,Da Rosa, Adriano,Flores, Alex F. C.,Zanatta, Nilo,Bonacorso, Helio G.

, p. 217 - 220 (2007/10/03)

A one-pot synthesis of 1-methyl- and 1-phenylpyrazole-3(5)-ethyl esters 2,3a-e by the cyclocondensation of β-alkoxyvinyl trichloromethyl ketones 1a- e with methyl and phenyl hydrazine hydrochloride under mild conditions, is reported. A study using compounds la-e with different substituents proved that these are versatile building blocks for the synthesis of pyrazole derivatives, having a 3(5)-ethoxycarbonyl substituent in good yields (60- 89%). The hydrazine and β-alkoxyvinyl trichloromethyl ketone substituent effects on the reaction regiochemistry on the formation of the 1,3- and 1,5- isomer were observed.

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